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An exploratory study on a new kidney-tonifying formula based on randomized, double-blind, placebo-controlled experiments.

An exploratory study on a new kidney-tonifying formula based on randomized, double-blind, placebo-controlled experiments.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025001853
Enrollment
Unknown
Registered
2025-09-26
Start date
2025-09-28
Completion date
Unknown
Last updated
2025-10-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Kidney Qi Deficiency Syndrome

Interventions

Treatment Group :Formulation I Group and Formulation II Group
Control Group:Therapeutically Inactive Placebo

Sponsors

Beijing University of Chinese Medicine Dongzhimen Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Gender unrestricted, meeting the diagnostic criteria for Kidney Qi Deficiency (excluding other types of kidney deficiency); 2. Aged between 18 and 70 years inclusive; 3. Voluntarily participate in this research study, sign the informed consent form, and agree to comply with the treatment.

Exclusion criteria

Exclusion criteria: ,: **Exclusion Criteria:** 1. Presence of concomitant severe cardiovascular, cerebrovascular, digestive, immune, or endocrine system diseases. 2. Presence of concomitant acute or infectious diseases. 3. Individuals with psychiatric disorders that preclude cooperation with the study. 4. Women who are pregnant, lactating, or planning pregnancy. 5. Patients participating in other clinical trials or currently taking health products with similar effects or those known to affect kidney function. 6. Individuals with chronic alcoholism or substance abuse. 7. Individuals with impairments in swallowing or drinking. 8. Individuals whose lifestyle, work, or transportation circumstances hinder their ability to attend follow-up visits. 9. Individuals with known allergies to any component of the investigational product.

Design outcomes

Primary

MeasureTime frame
Diagnostic Scale for Kidney Qi Deficiency Syndrome;

Secondary

MeasureTime frame
Diagnostic Scale for Male Reproductive Function;Diagnostic Scale for Female Reproductive Function;

Countries

China

Contacts

Public ContactYi Shi

Beijing University of Chinese Medicine Dongzhimen Hospital

docjoyshi@163.com13661152451

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Feb 4, 2026